CAS 1256360-42-5
:4-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
Description:
4-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a chemical compound characterized by its complex structure, which includes an indole moiety substituted with a chlorine atom and a boron-containing group. The presence of the chloro substituent indicates potential reactivity, particularly in nucleophilic substitution reactions. The tetramethyl-1,3,2-dioxaborolane group contributes to the compound's properties, enhancing its utility in organic synthesis, particularly in cross-coupling reactions such as Suzuki coupling. This compound may exhibit unique solubility characteristics due to the presence of both polar and nonpolar groups, influencing its behavior in various solvents. Additionally, the indole structure is known for its biological activity, which may suggest potential applications in pharmaceuticals or agrochemicals. Overall, the combination of these functional groups makes this compound of interest for researchers in synthetic organic chemistry and medicinal chemistry.
Formula:C15H19BClNO2
InChI:InChI=1S/C15H19BClNO2/c1-14(2)15(3,4)20-16(19-14)13-9-10-11(17)7-6-8-12(10)18(13)5/h6-9H,1-5H3
InChI key:InChIKey=VUBGUQRJVLABQU-UHFFFAOYSA-N
SMILES:CN1C(=CC=2C1=CC=CC2Cl)B3OC(C)(C)C(C)(C)O3
Synonyms:- 4-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
- 1H-Indole, 4-chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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Found 3 products.
4-Chloro-1-methylindole-2-boronic acid, pinacol ester
CAS:Formula:C15H19BClNO2Purity:96%Color and Shape:SolidMolecular weight:291.58094-Chloro-1-methylindole-2-boronic acid, pinacol ester
CAS:<p>4-Chloro-1-methylindole-2-boronic acid, pinacol ester</p>Purity:96%Molecular weight:291.58g/mol4-Chloro-1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
CAS:Purity:96%Molecular weight:291.5799866


